Micari Antonino, Bellocchi Paolo, Cautela Asya, Moncada Alice, Pluchino Matteo, Cusmà-Piccione Maurizio, Oreto Lilia, Vizzari Giampiero, Dattilo Giuseppe, Crea Pasquale
Cardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, AOU Policlinico "G. Martino", 98124 Messina, Italy.
Pediatric Cardiology Unit, Department of Clinical and Experimental Medicine, University of Messina, AOU Policlinico "G. Martino", 98124 Messina, Italy.
J Clin Med. 2025 Aug 21;14(16):5895. doi: 10.3390/jcm14165895.
Brugada syndrome (BrS) is a cardiac arrhythmic disorder associated with distinctive electrocardiographic (ECG) abnormalities and an increased risk of sudden cardiac death due to ventricular arrhythmias. While the classic BrS ECG pattern is a coved ST-segment elevation in the right precordial leads, a wide spectrum of atypical ECG presentations can mislead the diagnosis. This review discusses rare and under-recognized ECG findings associated with BrS, including its coexistence with right and left bundle branch block, alterations in peripheral leads and in the morphology of the QRS complex, as well as atrioventricular conduction abnormalities. Emphasis is placed on the clinical relevance of these findings, their underlying electrophysiological mechanisms, and their prognostic implications. Recognizing these atypical manifestations is critical to avoid misdiagnosing or failing to recognize the condition in patients with BrS.
布加综合征(BrS)是一种心律失常性疾病,与独特的心电图(ECG)异常相关,且因室性心律失常导致心脏性猝死的风险增加。虽然经典的布加综合征心电图模式是右胸前导联出现穹窿型ST段抬高,但广泛的非典型心电图表现可能会误导诊断。本综述讨论了与布加综合征相关的罕见且未被充分认识的心电图表现,包括其与右束支和左束支传导阻滞的共存、外周导联及QRS波群形态的改变,以及房室传导异常。重点阐述了这些表现的临床相关性、潜在的电生理机制及其预后意义。认识到这些非典型表现对于避免误诊或漏诊布加综合征患者至关重要。